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BOR - Papers in Press, published online ahead of print August 11, 2004.
Biol Reprod 2004, 10.1095/biolreprod.104.031831
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BIOLOGY OF REPRODUCTION 71, 1991–2002 (2004)
DOI: 10.1095/biolreprod.104.031831
© 2004 by the Society for the Study of Reproduction, Inc.


Ovary

Large-Scale Generation and Analysis of Expressed Sequence Tags from Porcine Ovary1

Honglin Jiang3,4, Kristin M. Whitworth4, Nathan J. Bivens4, James E. Ries4, Rami J. Woods4, Lawrence J. Forrester4, Gordon K. Springer4, Nagappan Mathialagan5, Cansu Agca4, Randall S. Prather4, and Matthew C. Lucy2,4

Department of Animal Science,4 University of Missouri, Columbia, Missouri 65211 Monsanto Company,5 St. Louis, Missouri 63198

One method to identify the factors that control ovarian function is to characterize the genes that are expressed in ovary. In the present study, cDNA libraries from fetal, neonatal, and prepubertal porcine ovaries, pubertal ovaries on different days of the estrous cycle (Days 0 [follicle], 5, and 12 [follicle and corpus luteum]), and follicles isolated from weaned sows (diameter, 2, 4, 6, and 8 mm) were constructed and sequenced. A total of 22 176 cDNAs were sequenced, of which 15 613 were of sufficient quality for clustering. Clustering of cDNAs resulted in 8507 contigs, 6294 (74%) of which were comprised of a single sequence. Sixty-eight percent of the contigs had consensus sequences that were homologous to existing Tentative Consensus (TC) sequences or mature transcripts (ET) in The Institute for Genomic Research Porcine Gene Index. The consensus sequences were classified according to the Gene Ontology Index. Most cDNA-encoded proteins were components of the nucleus, ribosome, or mitochondrion. The proteins primarily functioned in binding, catalysis, and transport. Nearly 75% of the proteins were involved in metabolism and cell growth and/or maintenance. Analysis of the cDNA frequency across different libraries demonstrated differential gene expression within different-size follicles, between follicles and corpora lutea, and across developmental time-points. The expression of selected genes (analyzed by ribonuclease protection assay and Northern blotting) was consistent with the frequency of their respective cDNA in the individual libraries. This porcine ovary unigene set will be useful for identifying factors and mechanisms controlling ovarian follicular development in a variety of species.

1 Supported in part by a grant from the Monsanto Company (St. Louis, MO) and the University of Missouri (Food for the 21st Century Program).

2 Correspondence: Matthew C. Lucy, 164 Animal Science Research Center, University of Missouri, Columbia, MO 65211. FAX: 573 882 6827; lucym{at}missouri.edu

3 Current address: Department of Animal and Poultry Sciences, Virginia Tech, Blacksburg, VA




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